NDC 62756-218 Ibandronate Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62756 - Sun Pharmaceutical Industries, Inc.
- 62756-218 - Ibandronate Sodium
Product Packages
NDC Code 62756-218-40
Package Description: 1 VIAL, SINGLE-DOSE in 1 CARTON / 3 mL in 1 VIAL, SINGLE-DOSE
Product Details
What is NDC 62756-218?
What are the uses for Ibandronate Sodium?
Which are Ibandronate Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBANDRONATE SODIUM (UNII: J12U072QL0)
- IBANDRONIC ACID (UNII: UMD7G2653W) (Active Moiety)
Which are Ibandronate Sodium Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ACETIC ACID (UNII: Q40Q9N063P)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Ibandronate Sodium?
- RxCUI: 904955 - ibandronate sodium 3 MG in 3 ML Injection
- RxCUI: 904955 - 3 ML ibandronic acid 1 MG/ML Injection
- RxCUI: 904955 - ibandronic acid 1 MG/ML (as ibandronate sodium 1.13 MG/ML) Injection
- RxCUI: 904955 - ibandronic acid 3 MG per 3 ML (as ibandronate sodium 1.13 MG/ML) Injection
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Patient Education
Ibandronate Injection
Ibandronate injection is used to treat osteoporosis (a condition in which the bones become thin and weak and break easily) in women who have undergone menopause (''change of life;'' end of menstrual periods). Ibandronate is in a class of medications called bisphosphonates. It works by preventing bone breakdown and increasing bone density (thickness).
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".